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Yumizen H500E CT

EUDAMED

Class B (EU MDR)

Ref 1300129763, 1300129764, 1300129765, 1300129766

by Horiba Abx Sas

Identity

Trade Name
Yumizen H500E CT EUDAMED
Device Name
Yumizen H500E CT EUDAMED
Model / Reference
1300129763, 1300129764, 1300129765, 1300129766 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230009567 EUDAMED
Basic UDI-DI
361023ymz_h500E_ctRV EUDAMED
EMDN Code
W0202010101 AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - LOW ROUTINE (Throughput <= 100 samples/hr) EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Yumizen H500E CT by Horiba Abx Sas — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (2)

  • EUDAMED 69521aca-0c63-4d22-b404-8b9d24328627 61 fields · synced Jun 18, 2026
  • EUDAMED 69521aca-0c63-4d22-b404-8b9d24328627-1 61 fields · synced Jun 9, 2026